» Articles » PMID: 30832275

Pharmacogenomic and Pharmacotranscriptomic Profiling of Childhood Acute Lymphoblastic Leukemia: Paving the Way to Personalized Treatment

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2019 Mar 6
PMID 30832275
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Personalized medicine is focused on research disciplines which contribute to the individualization of therapy, like pharmacogenomics and pharmacotranscriptomics. Acute lymphoblastic leukemia (ALL) is the most common malignancy of childhood. It is one of the pediatric malignancies with the highest cure rate, but still a lethal outcome due to therapy accounts for 1%⁻3% of deaths. Further improvement of treatment protocols is needed through the implementation of pharmacogenomics and pharmacotranscriptomics. Emerging high-throughput technologies, including microarrays and next-generation sequencing, have provided an enormous amount of molecular data with the potential to be implemented in childhood ALL treatment protocols. In the current review, we summarized the contribution of these novel technologies to the pharmacogenomics and pharmacotranscriptomics of childhood ALL. We have presented data on molecular markers responsible for the efficacy, side effects, and toxicity of the drugs commonly used for childhood ALL treatment, i.e., glucocorticoids, vincristine, asparaginase, anthracyclines, thiopurines, and methotrexate. Big data was generated using high-throughput technologies, but their implementation in clinical practice is poor. Research efforts should be focused on data analysis and designing prediction models using machine learning algorithms. Bioinformatics tools and the implementation of artificial i Lack of association of the CEP72 rs924607 TT genotype with intelligence are expected to open the door wide for personalized medicine in the clinical practice of childhood ALL.

Citing Articles

Acute Neurotoxicity in Children Treated for Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma: A 10-Year Single-Centre Experience.

Kranjcec I, Rajacic N, Janjic T, Kukuruzovic M, Jadrijevic-Cvrlje F, Pavlovic M Children (Basel). 2025; 12(1).

PMID: 39857862 PMC: 11763474. DOI: 10.3390/children12010031.


Unraveling the Genetic Heterogeneity of Acute Lymphoblastic Leukemia Based on NGS Applications.

Ramirez Maldonado V, Navas Acosta J, Maldonado Marcos I, Villaverde Ramiro A, Hernandez-Sanchez A, Hernandez Rivas J Cancers (Basel). 2024; 16(23).

PMID: 39682152 PMC: 11639785. DOI: 10.3390/cancers16233965.


Insights into Asparaginase Allergic Responses: Exploring Pharmacogenetic Influences.

Cecconello D, Silva K, de Senna E, Rechenmacher C, Daudt L, Michalowski M Pharmaceutics. 2024; 16(9).

PMID: 39339172 PMC: 11435241. DOI: 10.3390/pharmaceutics16091134.


The potential role of RNA sequencing in diagnosing unexplained insensitivity to conventional chemotherapy in pediatric patients with B-cell acute lymphoblastic leukemia.

Li X, Huang Z, Zhu L, Lai W, Li Y, Chen H BMC Med Genomics. 2024; 17(1):149.

PMID: 38811988 PMC: 11137891. DOI: 10.1186/s12920-024-01892-w.


A Review of Acute Lymphocytic Leukemia (ALL) in the Pediatric Population: Evaluating Current Trends and Changes in Guidelines in the Past Decade.

Ekpa Q, Akahara P, Anderson A, Adekoya O, Ajayi O, Alabi P Cureus. 2024; 15(12):e49930.

PMID: 38179374 PMC: 10766210. DOI: 10.7759/cureus.49930.


References
1.
Mizzi C, Dalabira E, Kumuthini J, Dzimiri N, Balogh I, Basak N . A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics. PLoS One. 2016; 11(9):e0162866. PMC: 5026342. DOI: 10.1371/journal.pone.0162866. View

2.
Ross C, Visscher H, Rassekh S, Castro-Pastrana L, Shereck E, Carleton B . Pharmacogenomics of serious adverse drug reactions in pediatric oncology. J Popul Ther Clin Pharmacol. 2011; 18:e134-51. View

3.
Chen S, Pei D, Yang W, Cheng C, Jeha S, Cox N . Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity. Clin Pharmacol Ther. 2010; 88(2):191-6. PMC: 3000799. DOI: 10.1038/clpt.2010.94. View

4.
Jamroziak K, Mlynarski W, Balcerczak E, Mistygacz M, Trelinska J, Mirowski M . Functional C3435T polymorphism of MDR1 gene: an impact on genetic susceptibility and clinical outcome of childhood acute lymphoblastic leukemia. Eur J Haematol. 2004; 72(5):314-21. DOI: 10.1111/j.1600-0609.2004.00228.x. View

5.
Schrappe M, Reiter A, Ludwig W, Harbott J, Zimmermann M, Hiddemann W . Improved outcome in childhood acute lymphoblastic leukemia despite reduced use of anthracyclines and cranial radiotherapy: results of trial ALL-BFM 90. German-Austrian-Swiss ALL-BFM Study Group. Blood. 2000; 95(11):3310-22. View